Evidence map›Paper›PMID 30044410›Full record

ArticleMolecules (Basel, Switzerland)2018

Histopathology of the Liver, Kidney, and Spleen of Mice Exposed to Gold Nanoparticles.

Khalid Elfaki Ibrahim, Mohsen Ghaleb Al-Mutary, Amel Omer Bakhiet, Haseeb Ahmad Khan

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 207 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  17. Comparative study for evaluation ofOpen veterinary journal · 2025
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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Khalid Elfaki IbrahimDepartment of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. kibrahim@ksu.edu.sa.
Mohsen Ghaleb Al-MutaryDepartment of Basic Sciences, College of Education, Imam Abdulrahman Bin Faisal University, Dammam 34212, Saudi Arabia. mgalmutary@iau.edu.sa.ORCID 0000-0002-9854-5230
Amel Omer BakhietDeanship of Scientific Research, Sudan University of Science and Technology, Khartoum 11111, Sudan. amel33@gmail.com.
Haseeb Ahmad KhanDepartment of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. haseeb@ksu.edu.sa.
King Saud University · SAImam Abdulrahman Bin Faisal University · SASudan University of Science and Technology · SD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gold nanoparticles (GNPs) are biocompatible nanomaterials that are currently researched for biomedical applications such as imaging and targeted drug delivery. In this investigation, we studied the effects of a single dose (injected on day 1) as well as a priming dose (two injections with a gap of one week) of 5 nm, 20 nm, and 50 nm diameter GNPs on the structural and biochemical changes in the liver, kidney, and spleen of mice. The results showed that small sized GNPs (5 nm) produced significant pathological changes in the liver on day 2 that gradually reduced on day 8. The medium (20 nm) and large (50 nm) sized GNPs preferentially targeted the spleen and caused significant pathological changes to the spleen architecture on day 2 that persisted on day 8 as well. There were minimal and insignificant pathological changes to the kidneys irrespective of the GNPs size. The animals that were primed with the pre-exposure of GNPs did not show any aggravation of histological changes after the second dose of the same GNPs. None of the dose regimens of the GNPs were able to significantly affect the markers of oxidative stress including glutathione (GSH) and malondialdehyde (MDA) in all of the organs that were studied. In conclusion, the size of GNPs plays an important role in their pathological effects on different organs of mice. Moreover, the primed animals become refractory to further pathological changes after the second dose of GNPs, suggesting the importance of a priming dose in medical applications of GNPs.

Indexed as

AnimalsDose-Response Relationship, DrugFemaleGlutathioneGoldKidneyLiverMalondialdehydeMetal NanoparticlesMiceOxidative StressParticle SizeSpleenSurface PropertiesTissue DistributionGlutathioneGoldMalondialdehydegold nanoparticleshistopathologykidneylivermicepriming dosespleen

Identifiers

PMID30044410
PMCPMC6222535
OpenAlexW2883360469

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.